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微流控技术中体细胞直接生成人类原始诱导多能干细胞。

Direct generation of human naive induced pluripotent stem cells from somatic cells in microfluidics.

机构信息

Department of Industrial Engineering, University of Padova, Padua, Italy.

Venetian Institute of Molecular Medicine, Padua, Italy.

出版信息

Nat Cell Biol. 2019 Feb;21(2):275-286. doi: 10.1038/s41556-018-0254-5. Epub 2018 Dec 31.

Abstract

Induced pluripotent stem cells (iPSCs) are generated via the expression of the transcription factors OCT4 (also known as POU5F1), SOX2, KLF4 and cMYC (OSKM) in somatic cells. In contrast to murine naive iPSCs, conventional human iPSCs are in a more developmentally advanced state called primed pluripotency. Here, we report that human naive iPSCs (niPSCs) can be generated directly from fewer than 1,000 primary human somatic cells, without requiring stable genetic manipulation, via the delivery of modified messenger RNAs using microfluidics. Expression of the OSKM factors in combination with NANOG for 12 days generates niPSCs that are free of transgenes, karyotypically normal and display transcriptional, epigenetic and metabolic features indicative of the naive state. Importantly, niPSCs efficiently differentiate into all three germ layers. While niPSCs can be generated at low frequency under conventional conditions, our microfluidics approach enables the robust and cost-effective production of patient-specific niPSCs for regenerative medicine applications, including disease modelling and drug screening.

摘要

诱导多能干细胞(iPS 细胞)是通过在体细胞中表达转录因子 OCT4(也称为 POU5F1)、SOX2、KLF4 和 cMYC(OSKM)而产生的。与鼠类原始 iPS 细胞不同,常规人类 iPS 细胞处于一种称为“初始状态”的更具发育潜力的状态。在这里,我们报告说,可以通过微流控技术使用修饰后的信使 RNA 直接从不到 1000 个人类原代体细胞中生成人类原始 iPS 细胞(niPS 细胞),而无需进行稳定的遗传操作。将 OSKM 因子与 NANOG 共同表达 12 天,可生成无转基因、染色体正常且表现出初始状态特征的转录组、表观遗传和代谢特征的 niPS 细胞。重要的是,niPS 细胞能够高效地分化为所有三个胚层。虽然 niPS 细胞在常规条件下以低频率生成,但我们的微流控方法可实现稳健且具有成本效益的患者特异性 niPS 细胞的生产,用于再生医学应用,包括疾病建模和药物筛选。

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